JPH09165454A - 予備成形されたケイ素変性有機ポリマーの架橋されたエマルジョン - Google Patents

予備成形されたケイ素変性有機ポリマーの架橋されたエマルジョン

Info

Publication number: JPH09165454A
Authority: JP; Japan
Prior art keywords: parts; group; silicon; polymer; groups
Prior art date: 1995-11-02
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.): Pending

Application number

JP8305489A

Other languages

English (en)

Japanese (ja)

Inventor

Eric Jude Joffre

ジュードジョフリーエリック

Arthur J Tselepis

ジェームズツェレピスアーサー

Andreas Thomas Franz Wolf

トーマスフランツボルフアンドレア

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Dow Silicones Corp

Original Assignee

Dow Corning Corp

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1995-11-02

Filing date

1996-11-01

Publication date

1997-06-24

1996-11-01 Application filed by Dow Corning Corp filed Critical Dow Corning Corp

1997-06-24 Publication of JPH09165454A publication Critical patent/JPH09165454A/ja

Status Pending legal-status Critical Current

Links

229920000620 organic polymer Polymers 0.000 title claims abstract description 207
239000000839 emulsion Substances 0.000 title claims abstract description 118
239000000203 mixture Substances 0.000 claims abstract description 202
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 91
239000004094 surface-active agent Substances 0.000 claims abstract description 51
125000003118 aryl group Chemical group 0.000 claims abstract description 16
238000004132 cross linking Methods 0.000 claims abstract description 11
XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims description 209
229910052710 silicon Inorganic materials 0.000 claims description 105
-1 siloxane unit Chemical group 0.000 claims description 103
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 65
150000001875 compounds Chemical class 0.000 claims description 54
239000010703 silicon Substances 0.000 claims description 53
239000006185 dispersion Substances 0.000 claims description 49
238000000034 method Methods 0.000 claims description 46
229910052799 carbon Inorganic materials 0.000 claims description 32
238000003756 stirring Methods 0.000 claims description 30
125000004432 carbon atom Chemical group C* 0.000 claims description 29
125000003342 alkenyl group Chemical group 0.000 claims description 11
125000000217 alkyl group Chemical group 0.000 claims description 11
125000001424 substituent group Chemical group 0.000 claims description 4
125000003710 aryl alkyl group Chemical group 0.000 claims description 2
230000009477 glass transition Effects 0.000 claims description 2
125000001183 hydrocarbyl group Chemical group 0.000 claims 1
230000001737 promoting effect Effects 0.000 claims 1
229920001971 elastomer Polymers 0.000 abstract description 38
239000000806 elastomer Substances 0.000 abstract description 38
239000000470 constituent Substances 0.000 abstract 1
229920000642 polymer Polymers 0.000 description 235
239000003054 catalyst Substances 0.000 description 145
239000004971 Cross linker Substances 0.000 description 128
239000003431 cross linking reagent Substances 0.000 description 102
230000005494 condensation Effects 0.000 description 60
238000009833 condensation Methods 0.000 description 59
KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 description 57
239000012071 phase Substances 0.000 description 54
238000006243 chemical reaction Methods 0.000 description 49
150000002430 hydrocarbons Chemical group 0.000 description 45
239000001257 hydrogen Substances 0.000 description 44
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238000009472 formulation Methods 0.000 description 41
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239000011347 resin Substances 0.000 description 37
239000007787 solid Substances 0.000 description 37
VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 34
125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 34
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239000004721 Polyphenylene oxide Substances 0.000 description 32
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239000011521 glass Substances 0.000 description 27
239000004816 latex Substances 0.000 description 27
BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 26
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 26
125000000524 functional group Chemical group 0.000 description 25
239000000945 filler Substances 0.000 description 24
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 22
229910008326 Si-Y Chemical group 0.000 description 22
229910006773 Si—Y Chemical group 0.000 description 22
238000013005 condensation curing Methods 0.000 description 22
125000003277 amino group Chemical group 0.000 description 21
229910018540 Si C Inorganic materials 0.000 description 20
229910010271 silicon carbide Inorganic materials 0.000 description 20
125000001951 carbamoylamino group Chemical group C(N)(=O)N* 0.000 description 19
238000002156 mixing Methods 0.000 description 19
239000000047 product Substances 0.000 description 19
230000007062 hydrolysis Effects 0.000 description 18
238000006460 hydrolysis reaction Methods 0.000 description 18
230000008569 process Effects 0.000 description 18
150000003839 salts Chemical class 0.000 description 18
125000003396 thiol group Chemical group [H]S* 0.000 description 18
229910000019 calcium carbonate Inorganic materials 0.000 description 17
150000001735 carboxylic acids Chemical class 0.000 description 17
229910052751 metal Inorganic materials 0.000 description 17
239000002184 metal Substances 0.000 description 17
LIVNPJMFVYWSIS-UHFFFAOYSA-N silicon monoxide Chemical compound [Si-]#[O+] LIVNPJMFVYWSIS-UHFFFAOYSA-N 0.000 description 17
229920001577 copolymer Polymers 0.000 description 16
238000004945 emulsification Methods 0.000 description 16
XYJRNCYWTVGEEG-UHFFFAOYSA-N trimethoxy(2-methylpropyl)silane Chemical compound CO[Si](OC)(OC)CC(C)C XYJRNCYWTVGEEG-UHFFFAOYSA-N 0.000 description 16
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 15
239000004698 Polyethylene Substances 0.000 description 15
229920000573 polyethylene Polymers 0.000 description 15
238000006459 hydrosilylation reaction Methods 0.000 description 13
229920001296 polysiloxane Polymers 0.000 description 13
ISKQADXMHQSTHK-UHFFFAOYSA-N [4-(aminomethyl)phenyl]methanamine Chemical compound NCC1=CC=C(CN)C=C1 ISKQADXMHQSTHK-UHFFFAOYSA-N 0.000 description 12
125000002344 aminooxy group Chemical group [H]N([H])O[*] 0.000 description 12
229910000077 silane Inorganic materials 0.000 description 12
238000007792 addition Methods 0.000 description 11
239000007859 condensation product Substances 0.000 description 11
IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 11
239000000178 monomer Substances 0.000 description 11
239000002736 nonionic surfactant Substances 0.000 description 11
239000013638 trimer Substances 0.000 description 11
125000004423 acyloxy group Chemical group 0.000 description 10
150000004808 allyl alcohols Chemical class 0.000 description 10
125000003368 amide group Chemical group 0.000 description 10
150000001721 carbon Chemical group 0.000 description 10
238000006482 condensation reaction Methods 0.000 description 10
239000000539 dimer Substances 0.000 description 10
CEIPQQODRKXDSB-UHFFFAOYSA-N ethyl 3-(6-hydroxynaphthalen-2-yl)-1H-indazole-5-carboximidate dihydrochloride Chemical group Cl.Cl.C1=C(O)C=CC2=CC(C3=NNC4=CC=C(C=C43)C(=N)OCC)=CC=C21 CEIPQQODRKXDSB-UHFFFAOYSA-N 0.000 description 10
230000036961 partial effect Effects 0.000 description 10
239000002245 particle Substances 0.000 description 10
239000000835 fiber Substances 0.000 description 9
239000012530 fluid Substances 0.000 description 9
229930195733 hydrocarbon Natural products 0.000 description 9
125000005372 silanol group Chemical group 0.000 description 9
229920002367 Polyisobutene Polymers 0.000 description 8
229960000583 acetic acid Drugs 0.000 description 8
125000003545 alkoxy group Chemical group 0.000 description 8
230000001804 emulsifying effect Effects 0.000 description 8
239000004615 ingredient Substances 0.000 description 8
SWGZAKPJNWCPRY-UHFFFAOYSA-N methyl-bis(trimethylsilyloxy)silicon Chemical compound C[Si](C)(C)O[Si](C)O[Si](C)(C)C SWGZAKPJNWCPRY-UHFFFAOYSA-N 0.000 description 8
125000003808 silyl group Chemical group [H][Si]([H])([H])[*] 0.000 description 8
239000000126 substance Substances 0.000 description 8
239000004215 Carbon black (E152) Substances 0.000 description 7
239000006263 elastomeric foam Substances 0.000 description 7
229910021485 fumed silica Inorganic materials 0.000 description 7
150000008282 halocarbons Chemical group 0.000 description 7
239000012948 isocyanate Substances 0.000 description 7
229920000728 polyester Polymers 0.000 description 7
229910052990 silicon hydride Inorganic materials 0.000 description 7
XSQUKJJJFZCRTK-UHFFFAOYSA-N urea group Chemical group NC(=O)N XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 7
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
150000001408 amides Chemical class 0.000 description 6
150000001412 amines Chemical class 0.000 description 6
239000003945 anionic surfactant Substances 0.000 description 6
RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 6
BFXIKLCIZHOAAZ-UHFFFAOYSA-N methyltrimethoxysilane Chemical compound CO[Si](C)(OC)OC BFXIKLCIZHOAAZ-UHFFFAOYSA-N 0.000 description 6
VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 6
239000000049 pigment Substances 0.000 description 6
239000000377 silicon dioxide Substances 0.000 description 6
239000002904 solvent Substances 0.000 description 6
150000003606 tin compounds Chemical class 0.000 description 6
239000002253 acid Substances 0.000 description 5
238000007259 addition reaction Methods 0.000 description 5
239000002318 adhesion promoter Substances 0.000 description 5
229910052783 alkali metal Inorganic materials 0.000 description 5
239000007864 aqueous solution Substances 0.000 description 5
239000003093 cationic surfactant Substances 0.000 description 5
239000008119 colloidal silica Substances 0.000 description 5
229920006037 cross link polymer Polymers 0.000 description 5
239000004205 dimethyl polysiloxane Substances 0.000 description 5
235000013870 dimethyl polysiloxane Nutrition 0.000 description 5
125000003700 epoxy group Chemical group 0.000 description 5
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 5
229920001002 functional polymer Polymers 0.000 description 5
239000007788 liquid Substances 0.000 description 5
150000002736 metal compounds Chemical class 0.000 description 5
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 5
229910000510 noble metal Inorganic materials 0.000 description 5
239000003960 organic solvent Substances 0.000 description 5
239000004014 plasticizer Substances 0.000 description 5
229920000435 poly(dimethylsiloxane) Polymers 0.000 description 5
238000002360 preparation method Methods 0.000 description 5
239000012763 reinforcing filler Substances 0.000 description 5
150000004756 silanes Chemical class 0.000 description 5
125000005625 siliconate group Chemical group 0.000 description 5
239000003381 stabilizer Substances 0.000 description 5
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 5
KWIUHFFTVRNATP-UHFFFAOYSA-O N,N,N-trimethylglycinium Chemical compound C[N+](C)(C)CC(O)=O KWIUHFFTVRNATP-UHFFFAOYSA-O 0.000 description 4
IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 4
ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 4
230000002411 adverse Effects 0.000 description 4
125000001931 aliphatic group Chemical group 0.000 description 4
239000002280 amphoteric surfactant Substances 0.000 description 4
239000002585 base Substances 0.000 description 4
229920001400 block copolymer Polymers 0.000 description 4
239000004202 carbamide Substances 0.000 description 4
150000001244 carboxylic acid anhydrides Chemical group 0.000 description 4
150000001732 carboxylic acid derivatives Chemical class 0.000 description 4
239000003795 chemical substances by application Substances 0.000 description 4
125000000753 cycloalkyl group Chemical group 0.000 description 4
235000014113 dietary fatty acids Nutrition 0.000 description 4
239000000194 fatty acid Substances 0.000 description 4
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150000002513 isocyanates Chemical class 0.000 description 4
229910052757 nitrogen Inorganic materials 0.000 description 4
229910017464 nitrogen compound Inorganic materials 0.000 description 4
150000002830 nitrogen compounds Chemical class 0.000 description 4
GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 4
125000000962 organic group Chemical group 0.000 description 4
125000001181 organosilyl group Chemical group [SiH3]* 0.000 description 4
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 4
230000000704 physical effect Effects 0.000 description 4
229920001451 polypropylene glycol Polymers 0.000 description 4
239000000565 sealant Substances 0.000 description 4
SCPYDCQAZCOKTP-UHFFFAOYSA-N silanol Chemical compound [SiH3]O SCPYDCQAZCOKTP-UHFFFAOYSA-N 0.000 description 4
239000002562 thickening agent Substances 0.000 description 4
CWERGRDVMFNCDR-UHFFFAOYSA-N thioglycolic acid Chemical compound OC(=O)CS CWERGRDVMFNCDR-UHFFFAOYSA-N 0.000 description 4
229910052718 tin Inorganic materials 0.000 description 4
150000004684 trihydrates Chemical class 0.000 description 4
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Chemical class CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 description 3
239000004593 Epoxy Substances 0.000 description 3
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 3
SJRJJKPEHAURKC-UHFFFAOYSA-N N-Methylmorpholine Chemical compound CN1CCOCC1 SJRJJKPEHAURKC-UHFFFAOYSA-N 0.000 description 3
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GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 3
239000012963 UV stabilizer Substances 0.000 description 3
238000012644 addition polymerization Methods 0.000 description 3
150000001335 aliphatic alkanes Chemical class 0.000 description 3
229910052782 aluminium Inorganic materials 0.000 description 3
PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 3
125000004103 aminoalkyl group Chemical group 0.000 description 3
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125000004429 atom Chemical group 0.000 description 3
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PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical compound C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 description 3
239000012011 nucleophilic catalyst Substances 0.000 description 3
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239000004848 polyfunctional curative Substances 0.000 description 3
150000003254 radicals Chemical class 0.000 description 3
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150000004760 silicates Chemical class 0.000 description 3
125000005373 siloxane group Chemical group [SiH2](O*)* 0.000 description 3
229910052708 sodium Inorganic materials 0.000 description 3
239000011734 sodium Substances 0.000 description 3
FVEFRICMTUKAML-UHFFFAOYSA-M sodium tetradecyl sulfate Chemical compound [Na+].CCCCC(CC)CCC(CC(C)C)OS([O-])(=O)=O FVEFRICMTUKAML-UHFFFAOYSA-M 0.000 description 3
230000003068 static effect Effects 0.000 description 3
125000003107 substituted aryl group Chemical group 0.000 description 3
PLFJWWUZKJKIPZ-UHFFFAOYSA-N 2-[2-[2-(2,6,8-trimethylnonan-4-yloxy)ethoxy]ethoxy]ethanol Chemical compound CC(C)CC(C)CC(CC(C)C)OCCOCCOCCO PLFJWWUZKJKIPZ-UHFFFAOYSA-N 0.000 description 2
PSBRNAUTQGUEPB-UHFFFAOYSA-N 2-[2-[2-(2-dodecoxyethoxy)ethoxy]ethoxy]ethyl dihydrogen phosphate Chemical compound CCCCCCCCCCCCOCCOCCOCCOCCOP(O)(O)=O PSBRNAUTQGUEPB-UHFFFAOYSA-N 0.000 description 2
229940058020 2-amino-2-methyl-1-propanol Drugs 0.000 description 2
125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 2
ALYNCZNDIQEVRV-UHFFFAOYSA-N 4-aminobenzoic acid Chemical compound NC1=CC=C(C(O)=O)C=C1 ALYNCZNDIQEVRV-UHFFFAOYSA-N 0.000 description 2
ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical group [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 2
QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
KWIUHFFTVRNATP-UHFFFAOYSA-N Betaine Natural products C[N+](C)(C)CC([O-])=O KWIUHFFTVRNATP-UHFFFAOYSA-N 0.000 description 2
VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 2
229920008712 Copo Polymers 0.000 description 2
RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 description 2
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
ZRALSGWEFCBTJO-UHFFFAOYSA-N Guanidine Chemical compound NC(N)=N ZRALSGWEFCBTJO-UHFFFAOYSA-N 0.000 description 2
XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 2
YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 2
239000005062 Polybutadiene Substances 0.000 description 2
KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 2
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QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 description 2
CQQXCSFSYHAZOO-UHFFFAOYSA-L [acetyloxy(dioctyl)stannyl] acetate Chemical compound CCCCCCCC[Sn](OC(C)=O)(OC(C)=O)CCCCCCCC CQQXCSFSYHAZOO-UHFFFAOYSA-L 0.000 description 2
KXJLGCBCRCSXQF-UHFFFAOYSA-N [diacetyloxy(ethyl)silyl] acetate Chemical compound CC(=O)O[Si](CC)(OC(C)=O)OC(C)=O KXJLGCBCRCSXQF-UHFFFAOYSA-N 0.000 description 2
TVJPBVNWVPUZBM-UHFFFAOYSA-N [diacetyloxy(methyl)silyl] acetate Chemical compound CC(=O)O[Si](C)(OC(C)=O)OC(C)=O TVJPBVNWVPUZBM-UHFFFAOYSA-N 0.000 description 2
VLFKGWCMFMCFRM-UHFFFAOYSA-N [diacetyloxy(phenyl)silyl] acetate Chemical compound CC(=O)O[Si](OC(C)=O)(OC(C)=O)C1=CC=CC=C1 VLFKGWCMFMCFRM-UHFFFAOYSA-N 0.000 description 2
UKLDJPRMSDWDSL-UHFFFAOYSA-L [dibutyl(dodecanoyloxy)stannyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCCCCCC UKLDJPRMSDWDSL-UHFFFAOYSA-L 0.000 description 2
XQBCVRSTVUHIGH-UHFFFAOYSA-L [dodecanoyloxy(dioctyl)stannyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCCCCCC)(CCCCCCCC)OC(=O)CCCCCCCCCCC XQBCVRSTVUHIGH-UHFFFAOYSA-L 0.000 description 2
NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
239000000654 additive Substances 0.000 description 2
239000000853 adhesive Substances 0.000 description 2
230000001070 adhesive effect Effects 0.000 description 2
125000005370 alkoxysilyl group Chemical group 0.000 description 2
125000005011 alkyl ether group Chemical group 0.000 description 2
150000008051 alkyl sulfates Chemical class 0.000 description 2
WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 2
CBTVGIZVANVGBH-UHFFFAOYSA-N aminomethyl propanol Chemical compound CC(C)(N)CO CBTVGIZVANVGBH-UHFFFAOYSA-N 0.000 description 2
QGZKDVFQNNGYKY-UHFFFAOYSA-O ammonium group Chemical group [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 2
150000008064 anhydrides Chemical class 0.000 description 2
230000003466 anti-cipated effect Effects 0.000 description 2
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239000003849 aromatic solvent Substances 0.000 description 2
125000005013 aryl ether group Chemical group 0.000 description 2
TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 2
230000008901 benefit Effects 0.000 description 2
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150000002085 enols Chemical class 0.000 description 1
150000002118 epoxides Chemical group 0.000 description 1
125000004185 ester group Chemical group 0.000 description 1
NKSJNEHGWDZZQF-UHFFFAOYSA-N ethenyl(trimethoxy)silane Chemical compound CO[Si](OC)(OC)C=C NKSJNEHGWDZZQF-UHFFFAOYSA-N 0.000 description 1
GBFVZTUQONJGSL-UHFFFAOYSA-N ethenyl-tris(prop-1-en-2-yloxy)silane Chemical group CC(=C)O[Si](OC(C)=C)(OC(C)=C)C=C GBFVZTUQONJGSL-UHFFFAOYSA-N 0.000 description 1
125000001033 ether group Chemical group 0.000 description 1
125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 1
XYIBRDXRRQCHLP-UHFFFAOYSA-N ethyl acetoacetate Chemical compound CCOC(=O)CC(C)=O XYIBRDXRRQCHLP-UHFFFAOYSA-N 0.000 description 1
229940093858 ethyl acetoacetate Drugs 0.000 description 1
SBRXLTRZCJVAPH-UHFFFAOYSA-N ethyl(trimethoxy)silane Chemical compound CC[Si](OC)(OC)OC SBRXLTRZCJVAPH-UHFFFAOYSA-N 0.000 description 1
229920006228 ethylene acrylate copolymer Polymers 0.000 description 1
238000001125 extrusion Methods 0.000 description 1
235000019197 fats Nutrition 0.000 description 1
229910052731 fluorine Inorganic materials 0.000 description 1
125000003709 fluoroalkyl group Chemical group 0.000 description 1
239000004088 foaming agent Substances 0.000 description 1
ISXSFOPKZQZDAO-UHFFFAOYSA-N formaldehyde;sodium Chemical compound [Na].O=C ISXSFOPKZQZDAO-UHFFFAOYSA-N 0.000 description 1
235000019253 formic acid Nutrition 0.000 description 1
239000007789 gas Substances 0.000 description 1
239000003365 glass fiber Substances 0.000 description 1
150000002314 glycerols Chemical class 0.000 description 1
239000010439 graphite Substances 0.000 description 1
229910002804 graphite Inorganic materials 0.000 description 1
150000004820 halides Chemical class 0.000 description 1
125000005843 halogen group Chemical group 0.000 description 1
WGXGAUQEMYSVJM-UHFFFAOYSA-N hexadecanenitrile Chemical compound CCCCCCCCCCCCCCCC#N WGXGAUQEMYSVJM-UHFFFAOYSA-N 0.000 description 1
125000006038 hexenyl group Chemical group 0.000 description 1
CZPWVGJYEJSRLH-UHFFFAOYSA-O hydron;pyrimidine Chemical compound C1=CN=C[NH+]=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-O 0.000 description 1
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
238000007373 indentation Methods 0.000 description 1
238000009776 industrial production Methods 0.000 description 1
229910052740 iodine Inorganic materials 0.000 description 1
229910052742 iron Inorganic materials 0.000 description 1
229940045996 isethionic acid Drugs 0.000 description 1
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
229940070765 laurate Drugs 0.000 description 1
229940094506 lauryl betaine Drugs 0.000 description 1
230000000670 limiting effect Effects 0.000 description 1
125000005647 linker group Chemical group 0.000 description 1
150000004668 long chain fatty acids Chemical class 0.000 description 1
231100000053 low toxicity Toxicity 0.000 description 1
VTHJTEIRLNZDEV-UHFFFAOYSA-L magnesium dihydroxide Chemical compound [OH-].[OH-].[Mg+2] VTHJTEIRLNZDEV-UHFFFAOYSA-L 0.000 description 1
239000000347 magnesium hydroxide Substances 0.000 description 1
229910001862 magnesium hydroxide Inorganic materials 0.000 description 1
229910052748 manganese Inorganic materials 0.000 description 1
239000011572 manganese Substances 0.000 description 1
150000002739 metals Chemical class 0.000 description 1
ARYZCSRUUPFYMY-UHFFFAOYSA-N methoxysilane Chemical class CO[SiH3] ARYZCSRUUPFYMY-UHFFFAOYSA-N 0.000 description 1
WTVDFNHBCFXARO-UHFFFAOYSA-N methyl sulfate;octadecylsulfanium Chemical compound COS([O-])(=O)=O.CCCCCCCCCCCCCCCCCC[SH2+] WTVDFNHBCFXARO-UHFFFAOYSA-N 0.000 description 1
DRXHEPWCWBIQFJ-UHFFFAOYSA-N methyl(triphenoxy)silane Chemical compound C=1C=CC=CC=1O[Si](OC=1C=CC=CC=1)(C)OC1=CC=CC=C1 DRXHEPWCWBIQFJ-UHFFFAOYSA-N 0.000 description 1
239000010445 mica Substances 0.000 description 1
229910052618 mica group Inorganic materials 0.000 description 1
239000004005 microsphere Substances 0.000 description 1
239000012778 molding material Substances 0.000 description 1
QOHMWDJIBGVPIF-UHFFFAOYSA-N n',n'-diethylpropane-1,3-diamine Chemical compound CCN(CC)CCCN QOHMWDJIBGVPIF-UHFFFAOYSA-N 0.000 description 1
PHQOGHDTIVQXHL-UHFFFAOYSA-N n'-(3-trimethoxysilylpropyl)ethane-1,2-diamine Chemical compound CO[Si](OC)(OC)CCCNCCN PHQOGHDTIVQXHL-UHFFFAOYSA-N 0.000 description 1
BLEJWUIEUACHKH-UHFFFAOYSA-N n-[[benzoyl(methyl)amino]-ethoxy-methylsilyl]-n-methylbenzamide Chemical compound C=1C=CC=CC=1C(=O)N(C)[Si](C)(OCC)N(C)C(=O)C1=CC=CC=C1 BLEJWUIEUACHKH-UHFFFAOYSA-N 0.000 description 1
XBFREHMGRPTPMU-UHFFFAOYSA-N n-[diacetamido(methyl)silyl]acetamide Chemical compound CC(=O)N[Si](C)(NC(C)=O)NC(C)=O XBFREHMGRPTPMU-UHFFFAOYSA-N 0.000 description 1
DVEKCXOJTLDBFE-UHFFFAOYSA-N n-dodecyl-n,n-dimethylglycinate Chemical compound CCCCCCCCCCCC[N+](C)(C)CC([O-])=O DVEKCXOJTLDBFE-UHFFFAOYSA-N 0.000 description 1
125000005609 naphthenate group Chemical group 0.000 description 1
229920001778 nylon Polymers 0.000 description 1
QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
UPHWVVKYDQHTCF-UHFFFAOYSA-N octadecylazanium;acetate Chemical compound CC(O)=O.CCCCCCCCCCCCCCCCCCN UPHWVVKYDQHTCF-UHFFFAOYSA-N 0.000 description 1
IOQPZZOEVPZRBK-UHFFFAOYSA-N octan-1-amine Chemical compound CCCCCCCCN IOQPZZOEVPZRBK-UHFFFAOYSA-N 0.000 description 1
XZZXKVYTWCYOQX-UHFFFAOYSA-J octanoate;tin(4+) Chemical class [Sn+4].CCCCCCCC([O-])=O.CCCCCCCC([O-])=O.CCCCCCCC([O-])=O.CCCCCCCC([O-])=O XZZXKVYTWCYOQX-UHFFFAOYSA-J 0.000 description 1
ZMHZSHHZIKJFIR-UHFFFAOYSA-N octyltin Chemical compound CCCCCCCC[Sn] ZMHZSHHZIKJFIR-UHFFFAOYSA-N 0.000 description 1
150000002894 organic compounds Chemical class 0.000 description 1
150000001282 organosilanes Chemical class 0.000 description 1
150000003961 organosilicon compounds Chemical class 0.000 description 1
150000002923 oximes Chemical class 0.000 description 1
TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
125000005702 oxyalkylene group Chemical group 0.000 description 1
229910052760 oxygen Inorganic materials 0.000 description 1
UJMWVICAENGCRF-UHFFFAOYSA-N oxygen difluoride Chemical compound FOF UJMWVICAENGCRF-UHFFFAOYSA-N 0.000 description 1
125000004817 pentamethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[*:1] 0.000 description 1
125000005496 phosphonium group Chemical group 0.000 description 1
239000004033 plastic Substances 0.000 description 1
150000003058 platinum compounds Chemical class 0.000 description 1
231100000572 poisoning Toxicity 0.000 description 1
230000000607 poisoning effect Effects 0.000 description 1
229920001084 poly(chloroprene) Polymers 0.000 description 1
229920006122 polyamide resin Polymers 0.000 description 1
229920001083 polybutene Polymers 0.000 description 1
229920001195 polyisoprene Polymers 0.000 description 1
238000006116 polymerization reaction Methods 0.000 description 1
229920000098 polyolefin Polymers 0.000 description 1
229920002635 polyurethane Polymers 0.000 description 1
239000004814 polyurethane Substances 0.000 description 1
230000035935 pregnancy Effects 0.000 description 1
HKJYVRJHDIPMQB-UHFFFAOYSA-N propan-1-olate;titanium(4+) Chemical compound CCCO[Ti](OCCC)(OCCC)OCCC HKJYVRJHDIPMQB-UHFFFAOYSA-N 0.000 description 1
239000010453 quartz Substances 0.000 description 1
230000005855 radiation Effects 0.000 description 1
239000002964 rayon Substances 0.000 description 1
230000009467 reduction Effects 0.000 description 1
230000002829 reductive effect Effects 0.000 description 1
230000002787 reinforcement Effects 0.000 description 1
230000004044 response Effects 0.000 description 1
239000006254 rheological additive Substances 0.000 description 1
238000012216 screening Methods 0.000 description 1
CDAISMWEOUEBRE-UHFFFAOYSA-N scyllo-inosotol Natural products OC1C(O)C(O)C(O)C(O)C1O CDAISMWEOUEBRE-UHFFFAOYSA-N 0.000 description 1
238000007493 shaping process Methods 0.000 description 1
150000004819 silanols Chemical class 0.000 description 1
125000005371 silicon functional group Chemical group 0.000 description 1
229920002050 silicone resin Polymers 0.000 description 1
239000002002 slurry Substances 0.000 description 1
159000000000 sodium salts Chemical class 0.000 description 1
229940074404 sodium succinate Drugs 0.000 description 1
ZDQYSKICYIVCPN-UHFFFAOYSA-L sodium succinate (anhydrous) Chemical compound [Na+].[Na+].[O-]C(=O)CCC([O-])=O ZDQYSKICYIVCPN-UHFFFAOYSA-L 0.000 description 1
241000894007 species Species 0.000 description 1
229910001220 stainless steel Inorganic materials 0.000 description 1
239000010935 stainless steel Substances 0.000 description 1
239000008117 stearic acid Substances 0.000 description 1
125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
238000003860 storage Methods 0.000 description 1
229920003048 styrene butadiene rubber Polymers 0.000 description 1
125000005156 substituted alkylene group Chemical group 0.000 description 1
150000005846 sugar alcohols Polymers 0.000 description 1
IIACRCGMVDHOTQ-UHFFFAOYSA-N sulfamic acid Chemical class NS(O)(=O)=O IIACRCGMVDHOTQ-UHFFFAOYSA-N 0.000 description 1
BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
238000006277 sulfonation reaction Methods 0.000 description 1
150000003460 sulfonic acids Chemical class 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
235000012222 talc Nutrition 0.000 description 1
ZQZCOBSUOFHDEE-UHFFFAOYSA-N tetrapropyl silicate Chemical compound CCCO[Si](OCCC)(OCCC)OCCC ZQZCOBSUOFHDEE-UHFFFAOYSA-N 0.000 description 1
LLZRNZOLAXHGLL-UHFFFAOYSA-J titanic acid Chemical class O[Ti](O)(O)O LLZRNZOLAXHGLL-UHFFFAOYSA-J 0.000 description 1
229910052719 titanium Inorganic materials 0.000 description 1
239000010936 titanium Substances 0.000 description 1
239000004408 titanium dioxide Substances 0.000 description 1
OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
ILJSQTXMGCGYMG-UHFFFAOYSA-N triacetic acid Chemical compound CC(=O)CC(=O)CC(O)=O ILJSQTXMGCGYMG-UHFFFAOYSA-N 0.000 description 1
FHVAUDREWWXPRW-UHFFFAOYSA-N triethoxy(pentyl)silane Chemical compound CCCCC[Si](OCC)(OCC)OCC FHVAUDREWWXPRW-UHFFFAOYSA-N 0.000 description 1
QQQSFSZALRVCSZ-UHFFFAOYSA-N triethoxysilane Chemical compound CCO[SiH](OCC)OCC QQQSFSZALRVCSZ-UHFFFAOYSA-N 0.000 description 1
125000000725 trifluoropropyl group Chemical group [H]C([H])(*)C([H])([H])C(F)(F)F 0.000 description 1
JLGNHOJUQFHYEZ-UHFFFAOYSA-N trimethoxy(3,3,3-trifluoropropyl)silane Chemical compound CO[Si](OC)(OC)CCC(F)(F)F JLGNHOJUQFHYEZ-UHFFFAOYSA-N 0.000 description 1
ZNOCGWVLWPVKAO-UHFFFAOYSA-N trimethoxy(phenyl)silane Chemical compound CO[Si](OC)(OC)C1=CC=CC=C1 ZNOCGWVLWPVKAO-UHFFFAOYSA-N 0.000 description 1
125000000026 trimethylsilyl group Chemical group [H]C([H])([H])[Si]([*])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
UGEBTGZCEBOXJS-UHFFFAOYSA-N trioctyltin Chemical compound CCCCCCCC[Sn](CCCCCCCC)(CCCCCCCC)[Sn](CCCCCCCC)(CCCCCCCC)CCCCCCCC UGEBTGZCEBOXJS-UHFFFAOYSA-N 0.000 description 1
PUMRXZLAGZFRGO-UHFFFAOYSA-N tris(2-ethoxyethoxy)-ethylsilane Chemical compound CCOCCO[Si](CC)(OCCOCC)OCCOCC PUMRXZLAGZFRGO-UHFFFAOYSA-N 0.000 description 1
GPRLSGONYQIRFK-MNYXATJNSA-N triton Chemical compound [3H+] GPRLSGONYQIRFK-MNYXATJNSA-N 0.000 description 1
150000003672 ureas Chemical class 0.000 description 1
JOYRKODLDBILNP-UHFFFAOYSA-N urethane group Chemical group NC(=O)OCC JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
239000010455 vermiculite Substances 0.000 description 1
229910052902 vermiculite Inorganic materials 0.000 description 1
235000019354 vermiculite Nutrition 0.000 description 1
239000000052 vinegar Substances 0.000 description 1
235000021419 vinegar Nutrition 0.000 description 1
KAKZBPTYRLMSJV-UHFFFAOYSA-N vinyl-ethylene Natural products C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 1
239000004636 vulcanized rubber Substances 0.000 description 1
210000002268 wool Anatomy 0.000 description 1
229910052725 zinc Inorganic materials 0.000 description 1
239000011701 zinc Substances 0.000 description 1
239000011787 zinc oxide Substances 0.000 description 1
MFFVROSEPLMJAP-UHFFFAOYSA-J zirconium(4+);tetraacetate Chemical compound [Zr+4].CC([O-])=O.CC([O-])=O.CC([O-])=O.CC([O-])=O MFFVROSEPLMJAP-UHFFFAOYSA-J 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J3/00—Processes of treating or compounding macromolecular substances
- C08J3/02—Making solutions, dispersions, lattices or gels by other methods than by solution, emulsion or suspension polymerisation techniques
- C08J3/03—Making solutions, dispersions, lattices or gels by other methods than by solution, emulsion or suspension polymerisation techniques in aqueous media
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G65/02—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
- C08G65/32—Polymers modified by chemical after-treatment
- C08G65/329—Polymers modified by chemical after-treatment with organic compounds
- C08G65/336—Polymers modified by chemical after-treatment with organic compounds containing silicon
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J3/00—Processes of treating or compounding macromolecular substances
- C08J3/24—Crosslinking, e.g. vulcanising, of macromolecules
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L101/00—Compositions of unspecified macromolecular compounds
- C08L101/02—Compositions of unspecified macromolecular compounds characterised by the presence of specified groups, e.g. terminal or pendant functional groups
- C08L101/10—Compositions of unspecified macromolecular compounds characterised by the presence of specified groups, e.g. terminal or pendant functional groups containing hydrolysable silane groups
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2300/00—Characterised by the use of unspecified polymers
- C08J2300/10—Polymers characterised by the presence of specified groups, e.g. terminal or pendant functional groups
- C08J2300/108—Polymers characterised by the presence of specified groups, e.g. terminal or pendant functional groups containing hydrolysable silane groups

Landscapes

Chemical & Material Sciences (AREA)
Health & Medical Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Organic Chemistry (AREA)
General Chemical & Material Sciences (AREA)
Dispersion Chemistry (AREA)
Compositions Of Macromolecular Compounds (AREA)
Silicon Polymers (AREA)
Inks, Pencil-Leads, Or Crayons (AREA)
Other Resins Obtained By Reactions Not Involving Carbon-To-Carbon Unsaturated Bonds (AREA)

JP8305489A 1995-11-02 1996-11-01 予備成形されたケイ素変性有機ポリマーの架橋されたエマルジョン Pending JPH09165454A (ja)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
US08/552162		1995-11-02
US08/552,162 US5840800A (en)	1995-11-02	1995-11-02	Crosslinked emulsions of pre-formed silicon modified organic polymers

Publications (1)

Publication Number	Publication Date
JPH09165454A true JPH09165454A (ja)	1997-06-24

Family

ID=24204182

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP8305489A Pending JPH09165454A (ja)	1995-11-02	1996-11-01	予備成形されたケイ素変性有機ポリマーの架橋されたエマルジョン

Country Status (9)

Country	Link
US (1)	US5840800A (fr)
EP (1)	EP0771855B1 (fr)
JP (1)	JPH09165454A (fr)
KR (1)	KR100304995B1 (fr)
CN (1)	CN1071349C (fr)
AU (1)	AU703181B2 (fr)
CA (1)	CA2189195A1 (fr)
DE (1)	DE69628714T2 (fr)
TW (1)	TW322499B (fr)

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JPH11193349A (ja) *	1997-10-09	1999-07-21	Dow Corning Corp	シリコーンラテックスの製造方法
JP2003522265A (ja) *	2000-02-11	2003-07-22	ダウ・コーニング・ソシエテ・アノニム	シリコーンポリマーエマルジョン
JP2018503724A (ja) *	2015-02-09	2018-02-08	ワッカーケミーアクチエンゲゼルシャフトＷａｃｋｅｒＣｈｅｍｉｅＡＧ	有機ケイ素化合物の水性分散液
JP2023173087A (ja) *	2022-05-25	2023-12-07	株式会社カネカ	硬化性組成物及びその硬化物

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EP1000979B1 (fr) *	1997-07-28	2009-05-13	Kaneka Corporation	Composition adhesive polymerisable
US6201064B1 (en) *	1997-11-06	2001-03-13	Kaneka Corporation	Crosslinked rubber particles, graft copolymer particles and thermoplastic resin composition
US6602964B2 (en) *	1998-04-17	2003-08-05	Crompton Corporation	Reactive diluent in moisture curable system
US6099971A (en) *	1998-09-09	2000-08-08	Plaskolite, Inc.	Polysiloxane abrasion and static resistant coating
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US6531210B1 (en)	1999-12-30	2003-03-11	United States Gypsum Company	Application of methylenediphenyldiisocyanate for producing gypsum/wood fiber board
US6569942B2 (en)	2001-03-14	2003-05-27	The Goodyear Tire & Rubber Company	Rubber compositions containing silicon coupled oligomers
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US6720373B2 (en) *	2001-07-13	2004-04-13	Dow Corning Corporation	High solids emulsions of curable elastomeric polymers
US6737473B2 (en) *	2001-07-13	2004-05-18	Dow Corning Corporation	High solids emulsions of elastomeric polymers
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US6713131B2 (en) *	2002-04-08	2004-03-30	Dow Corning Corporation	Methods of coating fabrics with emulsions of elastomeric polymers and polyurethane dispersions
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JP4101632B2 (ja)	2002-11-01	2008-06-18	株式会社カネカ	硬化性組成物および復元性、クリープ性改善方法
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US20040259991A1 (en) *	2003-06-17	2004-12-23	Weizhen Cai	Shelf-stable silane-modified aqueous dispersion polymers
US20040265531A1 (en) *	2003-06-30	2004-12-30	Mckean Dennis R.	Sliders bonded by a debondable silicon-based encapsulant
US7344783B2 (en) *	2003-07-09	2008-03-18	Shell Oil Company	Durable hydrophobic surface coatings using silicone resins
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US20080242744A1 (en) *	2003-07-23	2008-10-02	Kathleen Barnes	Process for making silicone-in-water emulsions
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US7183370B2 (en)	2003-09-11	2007-02-27	Toyota Technical Center Usa, Inc	Phosphonic-acid grafted hybrid inorganic-organic proton electrolyte membranes (PEMs)
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Publication number	Publication date
EP0771855A2 (fr)	1997-05-07
EP0771855A3 (fr)	1997-11-12
CA2189195A1 (fr)	1997-05-03
EP0771855B1 (fr)	2003-06-18
AU703181B2 (en)	1999-03-18
CN1071349C (zh)	2001-09-19
AU7055196A (en)	1997-05-08
DE69628714D1 (de)	2003-07-24
KR970027154A (ko)	1997-06-24
TW322499B (fr)	1997-12-11
DE69628714T2 (de)	2004-04-22
CN1151998A (zh)	1997-06-18
KR100304995B1 (ko)	2001-11-22
US5840800A (en)	1998-11-24

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